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Project Coordinator

Notice to Candidate: Location of this position is Shunyi, Beijing

JOB DESCRIPTIONS

1. To support the studies in the clinical planning and implementation of overall project plans, scopes, and schedules-ensuring deliverables are made on time and within project budget. Provide all assigned/clients support (as needed) throughout the duration of an assigned study. 支持臨床試驗項目整體項目計劃、范圍和時間表的規(guī)劃和實施，確保在項目預算內按時完成可交付成果。在特定項目的整個過程中（根據(jù)需要）完成指派任務/客戶支持。

2. Be instrumental in the delivery of services and manage the day-to-day study coordination work to meet the needs of clients. Act as a Day-to-day point of contact with client as part of the Project Team. 致力于提供服務，并管理日常項目協(xié)調工作，以滿足客戶的需求。作為項目團隊的一部分，擔當日常客戶聯(lián)系人。

3. Assist Project Managers and the Director, delivery in managing workflow and delivering on a wide variety of clients requests across assigned studies. 協(xié)助項目經理和總監(jiān)，管理工作流程，并在指定的研究中滿足各種客戶要求

4. Effectively communicate project expectations and status to team members and stakeholders in a timely and clear manner, and proactively manage changes in project scope, identify potential crises, and devise contingency plans. 及時、清晰地向團隊成員和利益干系人有效傳達項目期望和狀態(tài)，主動管理項目服務內容的變化，識別潛在的危機，制定應急計劃。

5. Develop and strengthen client relationships through demonstration of successful launches of study implementation. 通過成功啟動新項目來發(fā)展和加強客戶關系。

6. Strong to build, develop, and grow business relationships vital to the success of the project. 牢固地建立，發(fā)展和增長對項目成功至關重要的業(yè)務關系。

7. To support in foreseeing as many project-related risks that may occur, resolving conflicts and breaking down barriers throughout the process. 盡可能多地預見可能發(fā)生的與項目相關的風險，解決沖突并打破整個過程中的障礙。

EDUCATIONAL & QUALIFICATIONS

1. Bachelor's Degree is essential and in Life Sciences preferred.本科學歷以上，優(yōu)先考慮生命科學相關專業(yè)。

2. Have at least 1 year of experience as a Research Coordinator in a clinical research setting. OR 至少1年以上臨床研究領域研究協(xié)調員工作經驗。或

3. Have relevant experience working in clinical trials, either as a Site Coordinator or from the Sponsor or CRO side. OR擁有臨床試驗領域相關工作經驗，代表申辦方或CRO擔任現(xiàn)場協(xié)調員。或

4. Minimum 1 year of total experience in project/product coordination in the clinical trials industry or have additional certification for work Clinical Research such as Clinical Research Graduate Certificate, Good Documentary Practice (GDP), Research Ethics. 在臨床試驗業(yè)務領域1年以上項目/產品協(xié)調經驗或已獲得臨床試驗相關證書，如臨床試驗畢業(yè)證書、GDP，Research Ethics

5. Good command of communication skill and team player, integrity and honest. 良好的溝通協(xié)調能力和團隊合作能力，正直誠實。

6. Fluent in English reading and writing with average listening and speaking skills. 英語讀寫流利，聽說良好。